基础医学与临床 ›› 2026, Vol. 46 ›› Issue (6): 777-783.doi: 10.16352/j.issn.1001-6325.2026.06.0777

• 研究论文 • 上一篇    下一篇

HepaRG细胞自组织形成肝类器官的动态转录物组研究

夏婉娉, 保永莉, 李铭鸿, 吴汝成, 李书翔, 李雪媛, 陈阳*   

  1. 中国医学科学院北京协和医学院 基础医学研究所 生物化学与分子生物学系重大疾病共性机制研究全国重点实验室, 北京 100005
  • 收稿日期:2026-03-10 修回日期:2026-04-10 出版日期:2026-06-05 发布日期:2026-05-27
  • 通讯作者: *yc@ibms.pumc.edu.cn
  • 基金资助:
    国家自然科学基金(32570755);中国医学科学院医学与健康科技创新工程(2025-I2M-FGS-003)

Dynamic transcriptomic profiling during the self-organization of HepaRG cells into liver organoids

XIA Wanping, BAO Yongli, LI Minghong, WU Rucheng, LI Shuxiang, LI Xueyuan, CHEN Yang*   

  1. State Key Laboratory of Common Mechanism Research for Major Diseases, Department of Biochemistry and Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100005, China
  • Received:2026-03-10 Revised:2026-04-10 Online:2026-06-05 Published:2026-05-27
  • Contact: *yc@ibms.pumc.edu.cn

摘要: 目的 探讨HepaRG细胞三维培养形成肝类器官过程中0~120 h的时序性转录物组变化,解析增殖相关程序向分化及肝功能程序转换的分子特征。方法 HepaRG细胞与Matrigel按1∶1(v/v)混匀,接种超低吸附96孔板(5 000个细胞/孔)诱导形成类器官;于0 h、14 h、24 h、72 h和120 h取样成像并进行转录物组测序(RNA-seq)。对数据进行主成分分析(PCA)与相关性评估,采用DESeq2进行差异表达分析;对时间序列差异表达基因进行趋势聚类与功能富集,并构建蛋白质-蛋白质相互作用网络(PPI)分析关键模块。结果 三维培养下HepaRG细胞自组织形成球状类器官,白蛋白(ALB)表达上调;差异表达基因随时间增多,72~120 h最为显著。差异表达基因可分为6个时序簇,早期以增殖/细胞周期为主,晚期以肝功能相关通路(脂代谢、脂蛋白重塑、补体通路)增强为特征。结论 HepaRG类器官形成伴随显著的时序性转录物组重塑,72~120 h为肝功能相关程序增强的关键阶段,为类器官成熟评价与机制研究提供转录物组学依据。

关键词: HepaRG细胞, 肝类器官, 转录物组, 时间序列分析, 蛋白质-蛋白质相互作用网络

Abstract: Objective To investigate the time-dependent transcriptomic alterations during liver organoid formation from HepaRG cells under three-dimensional culture from 0 to 120 h, and to characterize molecular features associated with the programmatic transition from proliferation-related processes to hepatic functional differentiation. Methods HepaRG cells were mixed with Matrigel (1∶1, v/v) and seeded into ultra-low-attachment 96-well plates. Samples collected at 0 h, 14 h, 24 h, 72 h, and 120 h were subjected to RNA sequencing (RNA-seq), followed by principal component analysis (PCA)/correlation assessment, DESeq2-based differential expression, time-course clustering with enrichment analysis, and protein-protein interaction (PPI) network analysis. Results HepaRG cells self-assembled into spheroid organoids under three-dimensional culture, accompanied by increased albumin (ALB) expression. The number of differentially expressed genes (DEGs) peaked at 72 h and 120 h. Six temporal clusters revealed an early-to-late transition from proliferation/cell-cycle programs to hepatic functional programs (lipid metabolism, lipoprotein remodeling, and the complement pathway). Conclusions HepaRG organoid formation involves dynamic transcriptomic remodeling. The 72-120 h interval constitutes a critical stage with enhanced hepatic function-related programs, offering transcriptomic support for maturation evaluation and mechanistic studies.

Key words: HepaRG cells, liver organoids, transcriptome, time-series analysis, protein-protein interaction network

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